Evidence map›Paper›PMID 41562661›Full record

ArticleInfectious disease reports2026

Beyond the Skin: Topical Amphotericin B Nanocarriers Targeting Cutaneous Leishmaniasis with Suppression of Lymphatic Parasite Burden.

Francisco Alexandrino-Júnior, Gabriel Barcellos, Luiz Filipe Gonçalves-Oliveira, Luzia Monteiro de Castro Côrtes, Franklin Souza-Silva, Carlos Roberto Alves, Geovane Dias-Lopes, Juliana Figueiredo Peixoto, Beatriz Ferreira de Carvalho Patricio, Helvécio Vinícius Antunes Rocha

Abstract read
In one paragraph

Article in Infectious disease reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Francisco Alexandrino-JúniorLaboratório de Micro e Nanotecnologia, Centro de Desenvolvimento Tecnológico em Saúde (CDTS), Fundação Oswaldo Cruz, Avenida Brasil, 4036, Maré, Rio de Janeiro 21040-361, RJ, Brazil.ORCID 0000-0002-1173-9164
Gabriel BarcellosLaboratório de Micro e Nanotecnologia, Centro de Desenvolvimento Tecnológico em Saúde (CDTS), Fundação Oswaldo Cruz, Avenida Brasil, 4036, Maré, Rio de Janeiro 21040-361, RJ, Brazil.ORCID 0000-0002-3060-1355
Luiz Filipe Gonçalves-OliveiraLaboratório de Biologia Molecular e Doenças Endêmicas, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Avenida Brasil, 4365, Manguinhos, Rio de Janeiro 21040-900, RJ, Brazil.
Luzia Monteiro de Castro CôrtesLaboratório de Biologia Molecular e Doenças Endêmicas, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Avenida Brasil, 4365, Manguinhos, Rio de Janeiro 21040-900, RJ, Brazil.ORCID 0000-0003-3614-8763
Franklin Souza-SilvaLaboratório de Modelagem de Sistemas Biológicos, Centro de Desenvolvimento Tecnológico em Saúde, Fundação Oswaldo Cruz, Avenida Brazil, 4036, Manguinhos, Rio de Janeiro 21040-361, RJ, Brazil.ORCID 0000-0002-9216-4306
Carlos Roberto AlvesLaboratório de Biologia Molecular e Doenças Endêmicas, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Avenida Brasil, 4365, Manguinhos, Rio de Janeiro 21040-900, RJ, Brazil.ORCID 0000-0001-8703-426X
Geovane Dias-LopesLaboratório de Biologia Molecular e Doenças Endêmicas, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Avenida Brasil, 4365, Manguinhos, Rio de Janeiro 21040-900, RJ, Brazil.ORCID 0000-0003-4448-1398
Juliana Figueiredo PeixotoBiomedicina, Centro de Ciências da Saúde, Universidade Católica de Petrópolis, Rua Barão do Amazonas-124, Centro, Petrópolis 25685-100, RJ, Brazil.
Beatriz Ferreira de Carvalho PatricioLaboratório de Inovação Farmacêutica e Tecnológica, Instituto Biomédico, Universidade Federal do Estado do Rio de Janeiro (UNIRIO), Rio de Janeiro 20211-005, RJ, Brazil.ORCID 0000-0002-2477-9798
Helvécio Vinícius Antunes RochaLaboratório de Micro e Nanotecnologia, Centro de Desenvolvimento Tecnológico em Saúde (CDTS), Fundação Oswaldo Cruz, Avenida Brasil, 4036, Maré, Rio de Janeiro 21040-361, RJ, Brazil.ORCID 0000-0002-7914-5039

Funding

Federal University of State of Rio de Janeiro PPinst 2021Federal University of State of Rio de Janeiro PPinst 2022Federal University of State of Rio de Janeiro PPq 2022Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/010.000983/2019Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/200.2010/2023Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/200.799/2021Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/201.654/2021Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/204.189/2021National Council for Scientific and Technological Development 152770/2024-0National Council for Scientific and Technological Development 301744/2019-0
6 · The paper itself

Abstract

BACKGROUND/

objectivesCutaneous leishmaniasis (CL) remains a global health challenge, with treatment options often limited by drug resistance and systemic toxicity. Amphotericin B (AmB) represents a promising alternative. but intravenous administration causes severe systemic adverse effects. Despite growing interest in topical therapies, knowledge gaps remain regarding the comparative efficacy of delivery systems, including the influence of treatment timing and potential intrinsic effects. This study aimed to develop and characterize different topical AmB formulations (polymeric nanoparticles (PCL-AmB), a lipid-based (Oil_AmB) formulation, and a gel emulsion) to evaluate their in vivo efficacy against CL in a murine model, considering treatment initiation timing and potential intrinsic effects of the delivery systems.

methodsFormulations were prepared and characterized in terms of hydrodynamic size, polydispersity index, and AmB content. Antileishmanial activity was assessed in two independent in vivo experiments, with topical monotherapy administered five days per week for four weeks, starting either 10 or 30 days post-infection, representing early and established chronic stages of infection, respectively.

resultsAll formulations exhibited nanoscale dimensions and high homogeneity, with the lipid system demonstrating superior AmB solubilization. Both PCL-AmB and Oil_AmB reduced parasite load in the footpad, with Oil_AmB also reducing parasite load in draining lymph nodes.

conclusionsPCL-AmB and Oil_AmB reduced lesions and parasite burden in

Indexed as

lymph nodenanoparticleskin

Identifiers

PMID41562661
PMCPMC12821423

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.